Identifying and Preventing Overweight in Childhood Clinical Practice Guide Part II Fulltext Access 31 Pages 2006
Identifying and Preventing Overweight in Childhood Clinical Practice Guideline Part I Fulltext Access 31 Pages 2006
The Late Preterm Infant and the Control of Breathing, Sleep, and Brainstem Development: A Review Fulltext Access 32 Pages 2006
Pediatric Bipolar Disorder: Emerging Diagnostic and Treatment Approaches Fulltext Access 36 Pages 2006
Pharmacotherapy of Attention-Deficit Hyperactivity Disorder in Children and Adolescents: Update on New Stimulant Preparations, Atomoxetine, and Novel Treatments Fulltext Access 38 Pages 2006
Abstracts for the forthcoming International Federation of Placenta Associations Meeting Fulltext Access 57 Pages 2006
Abstracts: Joint Meeting, II Latinamerican Symposium on Fetal-Maternal Interaction and Placenta and XIX Anual Meeting of The Chilean Society of Physiological Sciences (SCHCF) Fulltext Access 72 Pages 2006
Abstracts of the 4th World Congress on Developmental Origins of Health and Disease (DOHaD), 13-16 September 2006, Educatorium, University of Utrecht, The Netherlands Fulltext Access 73 Pages 2006
Abstracts of Papers and Posters to Be Presented at the SOGC 62nd Annual Clinical Meeting/Résumé des Exposés et Affiches Qui Seront Présentés à la 62e Assemblée Clinique Annuelle Fulltext Access 79 Pages 2006
New horizons in the development of antiepileptic drugs: Innovative strategies Fulltext Access 90 Pages 2006
Focal seizure and cerebral contrast retention after cardiac catheterization Fulltext Access 4 Pages 2005
A case of psychosis with temporal lobe epilepsy: SPECT changes with treatment Fulltext Access 4 Pages 2005
Neonatal Seizures and Familial Hypomagnesemia With Secondary Hypocalcemia Fulltext Access 4 Pages 2005
Chorioamnionitis and Neonatal Encephalopathy in Term Infants With Fetal Acidemia: Histopathologic Correlations Fulltext Access 4 Pages 2005
Successful Treatment of Epilepsy and Celiac Disease With a Gluten-Free Diet Fulltext Access 4 Pages 2005
The Pharyngeal-Cervical-Brachial Form of Guillain-Barré Syndrome in Childhood Fulltext Access 4 Pages 2005
Clinical Heterogeneity in Familial Congenital Ptosis: Analysis of Fourteen Cases in One Family Over Five Generations Fulltext Access 4 Pages 2005
Efficacy of flunarizine in the prophylaxis of cyclical vomiting syndrome and abdominal migraine Fulltext Access 4 Pages 2005
EEG Evaluation of Fixation-Off Sensitivity in Eyelid Myoclonia With Absences Fulltext Access 4 Pages 2005
Pseudocystic cryptococcal meningitis complicated by transient periaqueductal obstruction in a child with HIV infection Fulltext Access 4 Pages 2005
Pancreatitis, complicated by a pancreatic pseudocyst associated with the use of valproic acid Fulltext Access 4 Pages 2005
Opsoclonus-myoclonus in an HIV-infected child on antiretroviral therapy-possible immune reconstitution inflammatory syndrome Fulltext Access 4 Pages 2005
Midbrain disconnection: An aetiology of severe central neonatal hypotonia Fulltext Access 4 Pages 2005
Bach flower remedies used for attention deficit hyperactivity disorder in children-A prospective double blind controlled study Fulltext Access 4 Pages 2005
Leukoencephalopathy around a tumor cyst following intracystic methotrexate injection Fulltext Access 4 Pages 2005
Treatment of electrical status epilepticus during slow-wave sleep with high-dose corticosteroid Fulltext Access 4 Pages 2005
Acute disseminated encephalomyelitis presenting with bilateral transient amaurosis Fulltext Access 4 Pages 2005
Changes in cerebral glucose metabolism in newborn infants with cerebral infarction Fulltext Access 4 Pages 2005
l-carnitine protects against glutamate- and kainic acid-induced neurotoxicity in cerebellar granular cell culture of rats Fulltext Access 4 Pages 2005
Longitudinal MR findings in a patient with hemimegalencephaly associated with tuberous sclerosis Fulltext Access 4 Pages 2005
Severe gastrointestinal dysmotility in a patient with congenital myopathy: causal relationship to decrease of interstitial cells of Cajal Fulltext Access 4 Pages 2005
Brown-Vialetto-Van Laere syndrome; variability in age at onset and disease progression highlighting the phenotypic overlap with Fazio-Londe disease Fulltext Access 4 Pages 2005
Coagulation system activated in Duchenne muscular dystrophy patients with cardiac dysfunction Fulltext Access 4 Pages 2005
Early onset myopathy with a novel mutation in the Selenoprotein N gene (SEPN1) Fulltext Access 4 Pages 2005
Tourette syndrome and chronic tics in a sample of children and adolescents Fulltext Access 4 Pages 2005
Symptoms related to ADHD observed in patients with pervasive developmental disorder Fulltext Access 4 Pages 2005
Postinfectious immune-mediated encephalitis after pediatric herpes simplex encephalitis Fulltext Access 4 Pages 2005
The effects of copper-histidine therapy on brain metabolism in a patient with Menkes disease: a proton magnetic resonance spectroscopic study Fulltext Access 4 Pages 2005
Modification of AMPA receptor properties following environmental enrichment Fulltext Access 4 Pages 2005
Delirious behavior in children with influenza: its clinical features and EEG findings Fulltext Access 4 Pages 2005
Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosis Fulltext Access 4 Pages 2005
Epilepsy and Intrathecal Baclofen Therapy in Children With Cerebral Palsy Fulltext Access 4 Pages 2005
CNS Siderosis and Dandy-Walker Variant After Neonatal Alloimmune Thrombocytopenia Fulltext Access 4 Pages 2005
Novel mutations in the thymidine kinase 2 gene (TK2) associated with fatal mitochondrial myopathy and mitochondrial DNA depletion Fulltext Access 4 Pages 2005
Antisense oligonucleotides in the treatment of Duchenne muscular dystrophy: Where are we now? Fulltext Access 4 Pages 2005
Transforming growth factor-β enhances connective tissue growth factor expression in L6 rat skeletal myotubes Fulltext Access 4 Pages 2005
ADAM12 overexpression does not improve outcome in mice with laminin α2-deficient muscular dystrophy Fulltext Access 4 Pages 2005
Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIE Fulltext Access 4 Pages 2005
Marked phenotypic variation in a family with a new myelin protein zero mutation Fulltext Access 4 Pages 2005
Major myofibrillar changes in early onset myopathy due to de novo heterozygous missense mutation in lamin A/C gene Fulltext Access 4 Pages 2005
Clinical features and neurophysiological follow-up in a case of Brown-Vialetto-Van Laere syndrome Fulltext Access 4 Pages 2005
Two patients with 'Dropped head syndrome' due to mutations in LMNA or SEPN1 genes Fulltext Access 4 Pages 2005
Peripheral nerve lesions associated with a dominant missense mutation, E33D, of the lamin A/C gene Fulltext Access 4 Pages 2005